A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615252



Internal ID16402661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:115490722..115552388hg38UCSC Ensembl
Innerchr9:118253001..118314667hg19UCSC Ensembl
Innerchr9:117292822..117354488hg18UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3861667
hg1961667
hg1861667
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1141281
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615252
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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